Canonical Allele Identifier: CA355378436
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777655G>T (hg19) chr3:g.184059867G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059867G>T , CM000665.2:g.184059867G>T GRCh38
NC_000003.11:g.183777655G>T , CM000665.1:g.183777655G>T GRCh37
NC_000003.10:g.185260349G>T NCBI36
NG_012749.1:g.11821G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.965G>T MANE Select ENSP00000322617.1:p.Ser322Ile
ENST00000318351.1:c.965G>T ENSP00000322617.1:p.Ser322Ile
NM_130770.2:c.965G>T NP_570126.2:p.Ser322Ile
NM_130770.3:c.965G>T MANE Select NP_570126.2:p.Ser322Ile
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